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Inherited macrocephaly-hamartoma syndromes

✍ Scribed by DiLiberti, John H.


Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
19 KB
Volume
79
Category
Article
ISSN
0148-7299
DOI
10.1002/(sici)1096-8628(19981002)79:4<284::aid-ajmg10>3.0.co;2-n

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✦ Synopsis


Recent discoveries in the molecular biology of the phosphatase and tensin homolog (PTEN) locus in the q22-23 region of chromosome 10 prove and/or suggest that several syndromes previously considered to be clinically and genetically distinct entities should actually be unified into a single entity. This conclusion is most secure for the Cowden and ''Bannayan-Zonana'' phenotypes, but almost certainly should also include the ''Riley-Ruvalcaba'' and Lhermitte-Duclos phenotypes as well benign familial macrocephaly and external hydrocephalus. The clinical and molecular data supporting this unification are presented along with a proposal for new nomenclature-the PTEN MATCHS (macrocephaly, autosomal dominant, thyroid disease, cancer, hamartomata, skin abnormalities) syndrome-based on the observed clinical abnormalities.


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